Canonical Allele Identifier: CA361039490
Gene: TGFBI HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136055717A>T , CM000667.2:g.136055717A>T GRCh38
NC_000005.9:g.135391406A>T , CM000667.1:g.135391406A>T GRCh37
NC_000005.8:g.135419305A>T NCBI36
NG_012646.1:g.31823A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000442011.7:c.1448A>T MANE Select ENSP00000416330.2:p.Asp483Val
ENST00000442011.6:c.1448A>T ENSP00000416330.2:p.Asp483Val
ENST00000506699.5:n.1965A>T
ENST00000507018.5:c.1426A>T
ENST00000509485.5:c.363A>T
ENST00000514242.5:n.219A>T
ENST00000514554.5:c.600A>T
NM_000358.2:c.1448A>T NP_000349.1:p.Asp483Val
NM_000358.3:c.1448A>T MANE Select NP_000349.1:p.Asp483Val